Kocostar Sun Block Capsule Mask

Manufacturer
Natuzen Co.,Ltd.
Effective date
2020-02-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:40:30

Label at a glance#

ProductKocostar Sun Block Capsule Mask
Active ingredientOCTINOXATE, OCTISALATE, TITANIUM DIOXIDE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: ETHYLHEXYL METHOXYCINNAMATE 7.5%, ETHYLHEXYL SALICYLATE 5.0%, TITANIUM DIOXIDE 3.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
Dimethicone, Cyclopentasiloxane, C12-15 Alkyl Benzoate, Polymethylsilsesquioxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Isoamyl p-Methoxycinnamate, Dimethicone/PEG-10/15 Crosspolymer, Dimethicone Crosspolymer, Aluminum Stearate, Alumina, Polyhydroxystearic Acid, Phenoxyethanol, Fragrance, Tocopheryl Acetate, Limonene, Linalool, Hexyl Cinnamal, Salicornia Herbacea Extract, Phragmites Communis Extract, Benzyl Benzoate, Butylphenyl Methylpropional, Citronellol, Butylene Glycol, Glycerin, Benzyl Alcohol, Citral, Benzyl Salicylate, 1,2-Hexanediol

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:
● For external use only.
● Use as directed.
● Stop using the product and consult a dermatologist or physician if the following occurs: -swelling, red (strawberry) marks, or other abnormalities -itchiness due to indirect or direct exposure to light
● Do not apply to open wounds, eczema, or dermatitis.
● Avoid contact with eyes. if contact occurs, flush eyes thoroughly with clean and warm water.

DESCRIPTION

DESCRIPTION SECTION

Uses:
Protect your skin from the Sun

Directions:
1. Twist off the tip of a heart-shaped sunscreen capsule.
2. Squeeze some amount of serum onto a fingertip.
3. Apply the serum to the skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of packageImage of package

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70930-10570930-105-01, 70930-105-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

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Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a73834aa-8a3e-47d8-b78f-c114366a58ee28b542f5-5582-4436-8802-7cc0b5f7fa5e2021-05-31WarningsExact identifier
spl set id: 28b542f5-5582-4436-8802-7cc0b5f7fa5e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.